scleroderma

Acute kidney injury of systemic sclerosis: scleroderma renal crisis and crescentic glomerulonephritis

系统性硬化并发急性肾损伤的临床病理分析

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The Cause of Scleroderma remains largely unknown.

硬皮病的发生原因很大方面还不是十分清楚.

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Scleroderma is a common disease in rheumatism.

硬皮病是自身免疫性疾病中的难治病.

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ABSTRACT: Objective To investigate the clinical characteristics of juvenile localized scleroderma ( JLS).

摘要：目的总结儿童局限性硬皮病的临床特点。

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However, there is increasingly strong evidence of a genetic predisposition to scleroderma.

然而, 存在硬皮病遗传因素的日益增长的证据.

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The structure and distribution of central nervous system of female Scleroderma sichuanensis were studied with dissecting microscope.

应用解剖镜研究了川硬皮肿腿蜂Scleroderma sichuanensis雌蜂中枢神经系统的结构与分布。

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Detection of collagen specific amino scids in scleroderma INSPECTION OF TEMPERATURE DIFFERENCE OF BUERGER'S DISEASE AND LOCALIZED SCLERODERMA WITH INFRARED THERMAL

硬皮病患者皮肤中胶原特异性氨基酸的测定分析红外热温差检测血栓闭塞性脉管炎与局限性硬皮病16例

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The cause of scleroderma is unknown.

硬皮病的原因尚不清楚.

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Sometimes scleroderma is caused by chemical or environmental exposures.

有些硬皮病可以由化学因素或环境因素造成的.

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Autoimmune: such as lupus erythematosus, rheumatoid arthritis, scleroderma, and other.

自身免疫性: 如红斑狼疮 、 类风湿关节炎 、 硬皮病等.

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Inspection of temperature difference of buerger's disease and localized scleroderma with infrared thermal

红外热温差检测血栓闭塞性脉管炎与局限性硬皮病16例

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The case was diagnosed as lichen sclerosus et atrophicus with localized scleroderma.

患者诊断为硬化萎缩性苔藓合并局限性硬皮病.

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Anti ScL 70 antibody has been used as a diagnostic marker of systemic scleroderma. ScL 70 is DNA topoisomerase ⅰ.

系统性硬化病是一种自身免疫病，抗ScL70抗体是该病的标记性抗体，其抗原ScL70就是DNA拓扑异构酶Ⅰ。

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Systemic Scleroderma is also known as Systemic Sclerosis.

系统性硬皮病也看作系统性硬化症.

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It discussed the preparing method of chromosome of Scleroderma sichuanensis ( Hymenoptera : Bethylidae Sclerderma )

对川硬皮肿腿蜂SclerodermasichuanensisXiao ( Hymenoptera:bethylidaeSclerderma ) 染色体制备方法进行了探讨,结果表明.

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Connective tissue disease ( CTD) includes many diseases. For instance, lupus erythematosus, scleroderma, rheumatoid arthritis, sjogren syndrome, dermatomyositis/ multiple myositis and vasculitis.

结缔组织病（CTD）包括许多种疾病，如红斑狼疮、硬皮病、类风湿关节炎、干燥综合征、皮肌炎/多发性肌炎及血管炎等。

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Necrobiosis lipoidica ( NL ) is a dermal tissue-involved disease characterized by scleroderma-like patches in the pretibial area.

类脂质渐进性 坏死 是发生在真皮结缔组织的疾病,以小腿胫前的硬皮病样斑块为临床特征.

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Its primary clinical manifestation is localized sclerosis of the skin, which is very similar to scleroderma.

该病和硬皮病的临床表现很相似,都是以局限性皮肤硬化为主要皮损表现.

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Autoimmune diseases and collagen diseases, such as systemic lupus erythematosus, dermatomyositis, scleroderma, and so on.

自身免疫性疾病及胶原性疾病, 如系统性红斑狼疮 、 皮肌炎 、 硬皮病等.

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It often affects various internal organs, such as lung, heart, kidney, and digestive tract, leading to severe complications such as pulmonary interstitial fibrosis and pulmonary hypertension. Ten-year survival rate of scleroderma is60%~ 90%.

此外，还可累及肺脏、心脏、肾脏、消化道等内脏器官，导致肺间质纤维化、肺动脉高压等严重并发症，10年生存率约为60%～90%。

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Conclusions Linear scleroderma are the most frequent subtype of JLS.

结论线状硬皮病是儿童局限性硬皮病中发病率最高的亚型。

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There was no cross reaction in the sera from 72 patients with dermatomyositis or polymyositis ( DM/ PM), from 48 patients with progressed systemic scleroderma ( PSS), and from 78 patients with mixed connective tissue disease ( MCTD).

对皮肌炎和多发性肌炎（DM/PM）72份、硬皮病（PSS）48份和混合性结缔组织病（MCTD）78份血清亦无交叉反应出现。

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Objective To explore the effect of Antisclerosis Composite Prescription ACP and penicillamine on scleroderma mouse.

目的探讨抗硬化复方与青霉胺对硬皮病小鼠模型的影响.

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Necrobiosis lipoidica ( NL) is a dermal connective tissue-involved disease characterized by scleroderma-like patches in the pretibial area.

类脂质渐进性坏死是发生在真皮结缔组织的疾病，以小腿胫前的硬皮病样斑块为临床特征。

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Visceral damage: in heart, lung lesions mainly accounted for60%, digestive system and heart, lung damage in diffuse cutaneous scleroderma and acral scleroderma in the distribution of no statistical significance.

内脏损害：以心、肺病变为主占60%，消化系统及心、肺的损害在弥漫皮肤型硬皮病及肢端型硬皮病中的分布无统计学意义。

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